Canonical Allele Identifier: PA2826634598
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2773636
ClinVar RCV Id: RCV003584492
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.His135Gln
CA346744359
NM_001281494.2:c.405C>A
CA346744363
NM_001281494.2:c.405C>G